Drug Elimination: Biopharmaceutics
Drug Elimination: Drug metabolism and basic understanding of metabolic pathways, renal excretion of drugs, factors affecting renal excretion of drugs, renal clearance, non-renal routes of drug excretion of drugs
Dr Alok Bains
9/13/20261 min read


Elimination: Drug metabolism and basic understanding of metabolic pathways, renal excretion of drugs, factors affecting renal excretion of drugs, renal clearance, and non-renal routes of drug excretion.
Elimination is an important pharmacokinetic process by which drugs and their metabolites are removed from the body. It helps terminate drug action and prevents excessive accumulation of drugs during repeated dosing. Elimination mainly occurs through drug metabolism and excretion. Drug metabolism, also called biotransformation, generally converts lipid-soluble drugs into more water-soluble compounds that can be eliminated more easily. Metabolic reactions are commonly classified into Phase I reactions such as oxidation, reduction and hydrolysis, and Phase II reactions such as conjugation. These reactions may occur mainly in the liver, although other tissues can also contribute.
The kidneys are the major organs responsible for renal excretion of drugs. Drugs are eliminated through the kidneys by three major processes: glomerular filtration, tubular secretion, and tubular reabsorption. Renal excretion is influenced by several factors, including renal blood flow, glomerular filtration rate, plasma protein binding, urine pH, drug lipid solubility, urinary flow, and the patient's age and renal function.
Renal clearance describes the volume of plasma from which a drug is completely removed by the kidneys per unit time. It is an important parameter for evaluating renal drug elimination and determining appropriate dosage regimens, particularly in patients with impaired renal function.
Apart from the kidneys, drugs may also be eliminated through non-renal routes, including the bile and faeces, lungs, saliva, sweat, tears, and breast milk. Understanding these pathways is essential for predicting drug disposition, duration of action, possible drug interactions and the risk of drug accumulation or toxicity.
https://drive.google.com/file/d/1QuPl7ocPtTZJ4jEW_RCwTQtTeYUwShVA/view?usp=drive_link
